|Publication number||US4826478 A|
|Application number||US 07/087,802|
|Publication date||May 2, 1989|
|Filing date||Aug 21, 1987|
|Priority date||Jun 23, 1986|
|Publication number||07087802, 087802, US 4826478 A, US 4826478A, US-A-4826478, US4826478 A, US4826478A|
|Original Assignee||Stanley Schocket|
|Export Citation||BiBTeX, EndNote, RefMan|
|Patent Citations (8), Non-Patent Citations (12), Referenced by (161), Classifications (7), Legal Events (3)|
|External Links: USPTO, USPTO Assignment, Espacenet|
This is a continuation in part application of U.S. Ser. No. 877,342, filed June 23, 1986, now U.S. Pat. No. 4,722,724 issued Feb. 2, 1988.
1. Field of the Invention
The present invention relates to an implant and a surgical technique for treating neovascular glaucoma, and particularly to improvements in the anterior chamber tube shunt to an encircling band procedure.
2. Description of Prior Art
Glaucoma, a disease of the eye which may ultimately cause blindness, is caused by increased intraocular pressure. Since as early as 1906, surgical techniques have been attempted to treat glaucoma by lowering intraocular pressure. A modern surgical technique has been described by Schocket et al, in an article entitled "Anterior Chamber Tube Shunt to an Encircling Band in the Treatment of Neovascular Glaucoma", Ophthalmology, Vol. 89, No. 10, pp. 1188-1194, 1982, and in another article entitled "Anterior Chamber Tube Shunt to an Encircling Band in the Treatment of neovascular Glaucoma and other Refractory Glaucomas", Ophthalmology, Vol. 92, No. 4, pp. 553-562, 1985.
According to the teachings of the above mentioned articles, aqueous is shunted from the anterior chamber of the eye to the orbit in order to reduce the intraocular pressure. The aqueous escapes through a tube inserted into the anterior chamber which is connected to a band which encircles the circumference of the eye. The aqueous fluid is shunted to an encapsulated reservoir and then diffuses through the capsular wall into the orbit to thereby lower the intraocular pressure.
Approximately two weeks after such surgery, the implanted materials become surrounded by a fibrous capsule separating the implant from the host tissue, a capsule that is contiguous with the tissue but not adherent to the implant. The capsule is apparently an attempt to destroy or isolate what the host tissue recognizes to be a foreign body. This encapsulation is essential for success and recovery in response to the surgical procedure.
Although this above-described work was a significant advance over the art, the implant of this surgical procedure can be improved. First, the surgically treated eye could be subject to bleeding into the anterior chamber. This could potentially occur at the time of insertion of the tube into the anterior chamber or shortly thereafter. As a consequence, blood clotting could occur which could block the opening in the tube needed to transport the aqueous from the eye, cause an increase in intraocular pressure, and render the procedure ineffective. This especially could occur in patients with severe rubeosis iridis.
An additional problem that could result with the known implant is that the patient could suffer from hypotony for a time period lasting from implantation until formation of the fibrous capsule around the implanted materials. Hypotony occurs when aqueous outflow from the chamber exceeds aqueous production as seen after insertion of the implant and causes too low an intraocular pressure and a corresponding flat anterior chamber. This could lead to further pathologic problems such as cataracts, adhesions of iris to cornea or lens, and in eyes which have had prior surgery, hemorrhagic choroidal detachments with a resultant loss of vision.
Further, although encapsulation of the implant is necessary for success of the surgical procedure, limiting the thickness of the capsule wall is desirable since this allows less restrictive movement of aqueous fluid out of the encircling band into the orbit and thereby ensures a good flow of aqueous. The known procedure did not possess this desired benefit.
Others have sought to remedy these problems, most notably the hypotony problem which occurs shortly after surgical implantation.
U.S. Pat. No. 3,788,327 to Donowitz et al disclose a surgical implant device. The Donowitz et al device is designed to rest on the surface of the cornea whereby a shank-like member with a valve to control intraocular pressure is mounted through the eye into the anterior chamber. Because the device is physically mounted onto the eye itself, friction occurs between the eyelid and the device. Additionally, the escaping aqueous flows to the cornea and not to the orbit. Furthermore, the valve in the Donowitz et al device must be permanently mounted in the shank to control the pressure in the anterior chamber.
U.S. Pat. No. 4,402,681 to Haas et al disclose an artificial implant valve. This valve is disadvantageous in that it is mounted into the posterior segment of the eye, and therefore it is difficult to adjust or remove the valve in the event of surgical complications. Further, the valve must remain permanently mounted to the eye to be effective. In addition, the construction of the valve in the Haas et al patent is composed of several parts and is complex.
Krupin et al disclosed valve implants for reducing intraocular pressure in an article entitled "Valve Implants in Filtering Surgery", American Journal of Opthalmology, Vol. 81, No. 2, pp. 232-235, 1976. The Krupin et al implant consists of a supramid tube which is cemented to a silastic tube. The end of the supramid tube is beveled and surgically inserted into the anterior chamber. The silastic tube remains outside the anterior chamber and has on its surface horizontal and vertical slits which function as a unidirectional valve. The Krupin et al device poses problems in that the valve is located in the silastic tube outside the anterior chamber. Therefore, if there are problems with the device, the conjunctiva and Tenon's Capsule must be surgically re-entered. Further, the device is designed so that the valve must be permanently mounted in the device if the device is to be effective.
Molteno et al also have developed a method of treating glaucoma. See Molteno et al, "Two Stage Insertion of Glaucoma Drainage Implants", Trans. Ophthal. Soc. N.Z., Vol. 31, pp. 17-26, 1979. According to the Molteno et al technique, a silicone tube is attached to a circular plate which is sutured to the globe. A silastic tube which is connected to the plate is sutured to the the sclera but is not inserted into the anterior chamber. Eight weeks later, a second operation is performed whereby the silastic tube is inserted into the anterior chamber. The Molteno et al procedure, therefore, requires two separate surgical operations to treat neovascular glaucoma and prevent hypotony.
White has disclosed a glaucoma pump shunt in "A New Implantable Ocular Pressure Relief Device: A Preliminary Report", Glaucoma, Vol. 7, pp. 289-294, 1985. The device consists of an inlet tube, an outlet tube, and a reservoir which connects the two tubes. Valves are located in both the inlet tube and the outlet tube, each valve located near the connecting reservoir. The end of the inlet tube located opposite from the connecting reservoir is mounted into the interior chamber. The reservoir is seated on the sclera and the posterior portion of the outlet tube is positioned in the sub-Tenon's space. This device is disadvantageous because of the intricate mounting of the reservoir and outlet tube, and because the inlet tube valve is located on the sclera and not in the anterior chamber, making it difficult to repair or replace the valve in case of failure. Additionally, because of the design of this system, the inlet and outlet valves are permanently mounted to the inlet and outlet tubes for the entire period when the device is implanted. Furthermore, the device is designed so that the reservoir permanently rests on the sclera and can potentially cause friction and erosion of the sclera and the conjunctive.
The inventor, in parent U.S. Application Ser. No. 877,342, filed June 23, 1986, prevents hypotony by utilizing a valve which takes the form of a temporary restriction. The valve is constructed so that it functions during the ten day to two week critical period when hypotony is most likely to occur. Thereafter, the valve is destroyed by a procedure such as a laser procedure, or the valve itself is made of a bio-destructible material such as collagen which automatically breaks down after the critical time period. Although this is an improvement upon existing technology, the presence of the restriction presents minor problems.
The problems associated with the restriction are two-fold. First, due to the nature of the restriction, the silastic tube attached to a silicone band can become completely clogged because of its reduced cross-sectional area. Moreover, additional means are necessary to ultimately destroy the valve after hypotony is no longer a risk.
Thus, a need exists for a simplified surgical procedure to treat glaucoma which may be performed in one step where the implanted device is easily accessible is follow-up surgery is needed to correct complications. Further, a need exists to prevent hypotony shortly after the surgical device is implanted without requiring the use of flow restricting means. Additionally, a need exists to regulate the volume of aqueous flowing from the anterior chamber and to ensure that aqueous flows from the chamber to thereby prevent a buildup of intraocular pressure. Further, a need exists to prevent bleeding associated with the surgical technique and to prevent clogging of the implant caused by blood clots located in the opening or within the lumen of the tube of the implant.
A purpose of the present invention is to provide a one-step surgical procedure whereby an implant is constructed by suturing one end of a silastic tube to a silicone band whereby the outer end of the silastic tube is mounted to be displaced away from the silicone band. The silicone band is positioned around the globe beneath the four rectus muscles of the eye. The displaced end of the silastic tube is then inserted via a needle tract into the anterior chamber under a scleral flap hinged at the limbus, defined by cauterizing the incision tract with a needle, inserting the needle into the anterior chamber and withdrawing it, injecting hyaluronic acid into the anterior chamber, and inserting the end of the silastic tube into the anterior chamber through a head of hyaluronic acid. The remainder of the silastic tube which is not mounted into the anterior chamber is mounted inside a groove of the silicone band with the grooved side facing the sclera when positioned around the eye. The silastic tube is sized lengthwise so that its length corresponds almost exactly to the length of the silicone band. By utilizing this length for the silastic tube, hypotony is controlled without requiring the use of a valve or flow restriction.
When the silicone band is sutured to the sclera of the eye, the orbit forms an encircling capsule around the implant where it has been mounted. Although this is necessary for the effective diffusion of aqueous into the orbit, it would be desirable to limit the density of the capsule wall since this would allow less restrictive movement of aqueous fluid out of the encircling reservoir and into the orbit. Therefore, all surfaces of the silastic tube and silicone band are coated with a heparin complex prior to surgical insertion to obtain a much less dense fibrous capsule. In addition to limiting the density of the capsule wall, the heparin serves to prevent the formation of clots along the aqueous pathway in contact with the implant.
Accordingly, it is an object of the present invention to provide an implant and a surgical technique to treat neovascular and other refractory glaucomas by reducing intraocular pressure in the anterior chamber without causing the patient to be subjected to dangerous side effects.
A further object of the present invention is to provide an implant and a surgical technique for treating neovascular and other refractory glaucomas whereby a sufficient pressure is maintained in the anterior chamber at the time of surgery and shortly thereafter to prevent hypotony.
A further object of the present invention is to provide an implant and a surgical procedure for treating neovascular and other refractory glaucomas whereby bleeding and blood clotting are minimized during and shortly after surgery.
An additional object of the present invention is to provide an implant and a surgical technique for treating aqueous from the anterior chamber to the orbit is maintained and whereby the body forms a thin walled fibrous capsule around the surgical implant.
Other objects and features of the present invention will become apparent to those skilled in the art when reference is made in the following description taken in conjunction with the accompanying drawings.
FIG. 1 is a view of a surgical implant which embodies the teachings of the instant invention.
FIG. 2 is a view of the surgical implant where the silicone band is positioned around the globe and where the silastic tube is located anteriorally just temporal to the superior rectus muscle.
FIG. 3 is a view of an eye before the surgical implant is inserted into the anterior chamber.
FIG. 4 is a view of an eye being treated with a cauterized needle before insertion of the silastic tube into the anterior chamber.
FIG. 5 is a view of the silastic tube being inserted into the anterior chamber.
FIG. 6 is a view of an eye after the silastic tube is inserted into the anterior chamber.
FIG. 7 is a view of the left eye and the right eye after completion of the inventive surgical procedure.
In describing the invention illustrated in the drawings, specific terminology will be resorted to for the sake of clarity. However, the invention is not intended tobe limited to the specific terms so selected, and it is to be understood that each specific term includes all technical equivalents which operate in a similar manner to accomplish a similar purpose.
Referring now to the drawings, and more particularly to FIG. 1, the basic elements of the inventive surgical implant are collectively designated as 10. Generally, implant 10 is constructed by mounting a silastic tube 22 to a silicone band 20. In the preferred embodiment of the present invention, silicone band 20 is a No. 20 type silicone band approximately 76 millimeters long and silastic tube 22 is 70 millimeters long, with an inside diameter of 0.30 millimeters and an outside diameter of 0.64 millimeters. In the preferred embodiment of the present invention, band 20 and tube 22 are both made of silicone polymers.
Silicone band 20 has a U-shaped groove 21 located at the center of one side and extending throughout the length of band 20. One end of tube 22 is placed in groove 21 and is fastened to band 20 by Supramyd sutures 28 or by any suitable equivalent.
The U-shaped groove 21 in silicone band 20 is defined by raised parallel sides 23 joined together by a groove bottom member. If the end of tube 22 which is mounted in groove 21 of band 20 becomes misaligned with groove 21 and intersects either side 23 allowing the tube end to touch with the episclera instead, fibrous tissue could encapsulate the intersection of tube 22 with side 23, block the opening of tube 22, and decrease the effectiveness of the implant. Therefore, it is important that tube 22 be securely mounted in the center of groove 21 to prevent encapsulation and clogging of tube 22.
To further secure the tube terminus, 3/4 of the inner wall of tube 22 is removed and the remaining tongue of silastic tube 22 is permanently secured to band 20 by a 5-0 Supramyd suture. The silicone band 20 inhibits fibrous ingrowth into silastic tube 22 only if tube remains in contact with band 20.
On one of raised sides 23 an indentation 25 is constructed by removing part of side 23. The end of tube 22 not secured in groove 21 is inserted in indentation 25 and is fastened to side 23 in indentation 25 by suture 28 or any other suitable fastening means.
The end of tube 22 which is mounted in indentation 25 of side 23 is obliquely cut to maximize the opening 24 of tube 22, which opening is designed to reside in the anterior chamber.
Insertion and operation of implant 10 is as follows. A 360° peritomy is made posterior and parallel to the limbus at the junction of cornea and sclera, except superiorly where the conjunctival incision is extended posteriorally. In the preferred embodiment of the surgical technique, the peritomy is made 4 to 5 millimeters posterior to the limbus and the conjunctival incision is extended posteriorally for 8 millimeters. A vitreous tap is performed if, despite pharmaceutical treatment, the intraocular pressure is equal to or greater than 40 millimeters of mercury. Traction sutures are then placed under the four rectus muscles.
Referring to FIGS. 2, 4, and 5, band 20 as illustrated is positioned so as to extend completely around the maximum circumference of the eye 30 (i.e., the equator), beneath the four rectus muscles 38, with groove 21 facing sclera 31. Band 20 is fastened to sclera 31 by fasteners such as sutures 35 (See FIGS. 4, 5) in the four quandrants such that the anterior edge of band 20 is located just posterior to the insertion of the rectus muscles. In the preferred surgical technique, the anterior edge is located approximately 10 to 12 millimeters from the limbus. The end of silastic tube 22 which is extended from band 20 should emerge from band 20 anteriorly, just temporal to the superior rectus. (See FIGS. 2, 4).
As FIGS. 2, 4 and 5 clearly show, tube 22 extends in groove 21 around the equator of the eye over nearly the entire length of the groove.
Referring to FIG. 3, a limbal based scleral flap 32 is raised and carried forward into the clear cornea. According to the preferred surgical technique, the flap measures 4 millimeters by 4 millimeters and is carried forward one millimeter into the clear cornea. Tube 22 is then anchored to the posterior and temporal edges of the scleral bed so that, on insertion, tube 22 lies over the nasal iris. In the preferred surgical technique utilized when practicing the invention, anchoring is accomplished by 10-0 nylon sutures.
Entry to anterior chamber 40 is effected first by directing a needle 34 into anterior chamber 40 (See FIG. 4). In the preferred surgical technique, the needle is 25-gauge (0.5 mm outside diameter) and is bent to allow entry parallel to the iris. To prevent bleeding caused by entry of the needle 34 into a highly neovascularized angle, needle 34 is touched with a wet-field cautery to obtain coagulation of the ruptured bleeding angle vessels upon insertion. On withdrawal of needle 34, anterior chamber 40 becomes shallow due to loss of aqueous. Hyaluronic acid (Healon®) is injected into anterior chamber 40 through a 23-gauge needle (0.65 mm outside diameter) to restore anterior chamber 40 with hyaluronic acid. In the preferred surgical technique, 0.1 to 0.3 milliliters of hyaluronic acid is injected to deepen the chamber to full depth. The needle is removed from the anterior chamber 40 and the hyaluronic acid refluxes to form a bead 36 which indicates the opening to the anterior chamber 40 (see FIG. 5).
The end of tube 22 lying over the nasal iris is compressed between the jaws of a microforceps 41 (see FIG. 5), and is introduced into anterior chamber 40 by insertion through bead 36. Tube 22 is inserted into anterior chamber 40 until the desired length of tube 22 has entered the chamber (See FIG. 6). According to the preferred surgical technique utilized when practicing the present invention, the tube should extend approximately 3 millimeters into the anterior chamber.
Scleral flap 32 is then closed by suitable means such as nylon sutures located at the two posterior corners. (See FIG. 7). Scleral flap 32 is made slightly temporal to the mid-line in each eye to allow coverage of silastic tube 22, which is angled towards the nasal iris. Tenon's capsule over the tube is closed separately from the conjunctiva by suitable means such as a running 7-Vicryl suture. The conjunctiva is then closed by a suitable means such as a continuous 6-0 plain cat gut suture. 40 mg of Gentamicin sulfate and 4 mg of dexamethasone phosphate are injected into the inferior subconjunctival space to complete the surgical technique.
This procedure results in the formation of a fibrous capsule surrounding silicone band 20. The capsule forms within ten days to two weeks after implantation and is apparently an attempt of the body to destroy or isolate what the host tissue recognizes to be a foreign substance, namely, silicone band 20. Aqueous fluid draining from anterior chamber 40 through tube 22 into band 20 is known to diffuse into and expand this capsule. Fibrous encapsulation of silicone band 20 is essential for the success of the surgical procedure because the capsule acts as the wall of the reservoir through which aqueous diffuses into the orbit to be picked up by orbital vessels which return the fluid to the general blood circulation.
To prevent hypotony from occurring during the formation of the fibrous capsule, tube 22 is sized to that its length approximates the length of band 20. For a typical human eye, the circumference of the eye is approximately 74 mm. Thus, the length of band 20 is approximately 76 mm.
The production of aqeous by the eye is approximately 2.54 microliters of aqueous per minute. In the past, such as the implant disclosed in U.S. Ser. No. 877,342, the length of tube 22 was approximately 30 mm. By utilizing this length, the rate of diffusion of aqueousf romthe anterior chamber to the silicone band was approximately 5.86 microliters per minute at a pressure of 18 mm of Hg. This flow rate would cause hypotony as the anterior chamber would tend to flatten. Thus, as discussed above, a restriction was necessary to limit the flow rate.
In the present invention, it was discovered that if the length of tube 22 would approximate the length of band 20, the flow rate of aqueous from the anterior chamber would be reduced to 3.54 microliters per minute at 18 mm of Hg. This flow rate is signficiantly low enough to prevent hypotony as the anterior chamber would not flatten due to the loss of aqueous. Moreover, this flow rate is established without requiring the use of a flow restriction. Rather, it is the length of tube 22 which causes this remarkable decrease in flow of aqueous.
To limit the density of the fibrous capsule walls (i.e., to maximize fluid flow and prevent clotting), a more bioreactive silicone implant may be inserted. One such method of creating a more bioreactive silicone implant is to fix a heparin complex to the silicone polymer.
Heparin, a substance normally found in ocular tissues, is an acid mucopolysaccharide or glycosaminoglycan, and is therefore a mroe bioreactive material than a silicone polymer. The heparin fixing process consists of immersing implant 10 in a solution of heparin-quaternary ammonium compound-complex in an organic solvent, removing the organic solvent, and sterilizing by gas or heat. The amount of complex fixed to all surfaces of implant 10 is approximately 40 mg/cm2 ; the surface concentration is controlled by the concentration of the complex and the duration of the immersion.
The complex between heparin and tridodecylmethylammonium chloride (TDMAC) is formed when heparin, an acid mucopolysaccharide with an overall negative charge, is exposed to the TDMAC ammonium ion which is positively charged. ##STR1##
To effectively coat tube 22 and band 20 with a heparin solution, all surfaces of tube 22 and band 20 are treated with a one percent solution of the Heparin-TDMAC complex in 1:1 toluene/petroleum ether at room temperature for 30-60 seconds. Tube 22 and band 20 are then flushed with compressed air, and dried overnight in a vacuum oven to remove traces of the volatile organic solvent.
During the immersion process, the surface of the silicone polymer is swollen by the organic solvent, allowing penetration of the polymer surface by the hydrophobic hydrocarbon chains of the TDMAC portion of the complex. Removal of the organic solvent by evaporation results in firm fixation of the complex to the polymer surface as the polymer shrinks back to normal size. The surface-bound complex on polymers such as the present silicone implant is resistant to elution by saline or blood. Surface-bound heparin apparently causes thromboresistance in the same way as heparin does in solution. The presence of a heparin complex on the surface of silicone polymers probably simulates the naturally occurring heparin coat of the endothelium, thereby decreasing protein, leukocyte and platelet adherence, and resulting in prolonged coagulation time.
The heparin coating to all surfaces of tube 22 and band 20 effectively reduces the thickness of the fibrous capsule because the coating prevents the host tissue from fully recognizing the implant as a foreign body, and thus allows aqueous to flow through tube 22 into band 20 and diffuse through band 20 to the encapsulating fibrous tissue more rapidly.
Further, the heparin coating of silastic tube 22, acts to prevent tube obstruction by blood clots. A low intraocular pressure of 10 mm Hg is capable of flushing blood from heparinized tube 22 in 1 to 2 seconds whereas in a non-heparinized tube the intraocular pressure must be 60 mm Hg to flush the tube. If blood remains in the non-heparinized tube for 30 minutes, a pressure of 60 mm Hg is incapable of flushing the tube whereas in heparinized tube 22 the clot is expelled after 2 seconds.
From the above, it should be apparent that many modifications and variations of the present invention are possible. It is therefore to be understood that, within the scope of the appended claims, the invention may be practiced otherwise than as specifically described.
|Cited Patent||Filing date||Publication date||Applicant||Title|
|US3736939 *||Jan 7, 1972||Jun 5, 1973||Kendall & Co||Balloon catheter with soluble tip|
|US3788327 *||Mar 30, 1971||Jan 29, 1974||Donowitz H||Surgical implant device|
|US3976081 *||Apr 10, 1974||Aug 24, 1976||Abraham Lapidot||Laminar middle ear vent tube assembly|
|US4249535 *||Feb 2, 1979||Feb 10, 1981||Hargest Thomas S Iii||Gastric feeding device|
|US4402681 *||Sep 10, 1981||Sep 6, 1983||Haas Joseph S||Artificial implant valve for the regulation of intraocular pressure|
|US4457757 *||Jul 20, 1981||Jul 3, 1984||Molteno Anthony C B||Device for draining aqueous humour|
|US4554918 *||Jul 28, 1982||Nov 26, 1985||White Thomas C||Ocular pressure relief device|
|US4604087 *||Jun 21, 1985||Aug 5, 1986||Joseph Neil H||Aqueous humor drainage device|
|1||*||Hufnagel et al., Surgery, vol. 61, No. , pp. 11 16, 623 2, Jan. 1967.|
|2||Hufnagel et al., Surgery, vol. 61, No. , pp. 11-16, 623-2, Jan. 1967.|
|3||Krupin et al, "Valve Implants in Filtering Surgery," American Journal of Ophthalmology, vol. 81, pp. 232-235, 1976.|
|4||*||Krupin et al, Valve Implants in Filtering Surgery, American Journal of Ophthalmology, vol. 81, pp. 232 235, 1976.|
|5||Molteno et al., "Two-Stage Insertion of Glaucoma Drainage Implant," Trans. Opthal. Soc. N.Z., 31, pp. 17-26, 1979.|
|6||*||Molteno et al., Two-Stage Insertion of Glaucoma Drainage Implant, Trans. Opthal. Soc. N.Z., 31, pp. 17 26, 1979.|
|7||Schocket et al., "Anterior Chamber Tube Shunt to an Encircling band in the Treatment of Neovascular Glaucoma and Other Refractory Glaucomas," Ophthalmology 92, pp. 553-562, 1985.|
|8||Schocket et al., "Anterior Chamber Tube Shunt to an Encircling Band in the Treatment of Neovascular Glaucoma," Ophthalmology 89, pp. 1188-1194, 1982.|
|9||*||Schocket et al., Anterior Chamber Tube Shunt to an Encircling band in the Treatment of Neovascular Glaucoma and Other Refractory Glaucomas, Ophthalmology 92, pp. 553 562, 1985.|
|10||*||Schocket et al., Anterior Chamber Tube Shunt to an Encircling Band in the Treatment of Neovascular Glaucoma, Ophthalmology 89, pp. 1188 1194, 1982.|
|11||White, "A New Implantable Ocular Pressure Relief Device: A Preliminary Report," Glaucoma, 7, pp. 289-294, 1985.|
|12||*||White, A New Implantable Ocular Pressure Relief Device: A Preliminary Report, Glaucoma, 7, pp. 289 294, 1985.|
|Citing Patent||Filing date||Publication date||Applicant||Title|
|US5092837 *||Aug 27, 1990||Mar 3, 1992||Robert Ritch||Method for the treatment of glaucoma|
|US5370607 *||Oct 28, 1992||Dec 6, 1994||Annuit Coeptis, Inc.||Glaucoma implant device and method for implanting same|
|US5411473 *||Oct 1, 1991||May 2, 1995||Ahmed; A. Mateen||Medical valve|
|US5433701 *||Dec 21, 1994||Jul 18, 1995||Rubinstein; Mark H.||Apparatus for reducing ocular pressure|
|US5454796 *||Mar 10, 1993||Oct 3, 1995||Hood Laboratories||Device and method for controlling intraocular fluid pressure|
|US5462739 *||Nov 16, 1992||Oct 31, 1995||Yeda Research And Development Co., Ltd.||Microdelivery device and method for enhanced drug administration to the eye|
|US5486165 *||Jan 13, 1994||Jan 23, 1996||Stegmann; Robert||Method and appliance for maintaining the natural intraocular pressure|
|US5520631 *||Jul 22, 1994||May 28, 1996||Wound Healing Of Oklahoma||Method and apparatus for lowering the intraocular pressure of an eye|
|US5626558 *||May 5, 1995||May 6, 1997||Suson; John||Adjustable flow rate glaucoma shunt and method of using same|
|US5652014 *||Aug 13, 1992||Jul 29, 1997||Galin; Miles A.||Medicament coated refractive anterior chamber ocular implant|
|US5702414 *||Sep 5, 1996||Dec 30, 1997||Optonol Ltd||Method of implanting an intraocular implant|
|US5704907 *||Dec 11, 1995||Jan 6, 1998||Wound Healing Of Oklahoma||Method and apparatus for lowering the intraocular pressure of an eye|
|US5713844 *||Jan 10, 1997||Feb 3, 1998||Peyman; Gholam A.||Device and method for regulating intraocular pressure|
|US5868697 *||Mar 27, 1996||Feb 9, 1999||Optonol Ltd.||Intraocular implant|
|US5944753 *||Mar 12, 1997||Aug 31, 1999||Galin; Miles A.||Medicament coated refractive anterior chamber ocular implant|
|US5968058 *||Jul 14, 1997||Oct 19, 1999||Optonol Ltd.||Device for and method of implanting an intraocular implant|
|US6007511 *||May 8, 1991||Dec 28, 1999||Prywes; Arnold S.||Shunt valve and therapeutic delivery system for treatment of glaucoma and methods and apparatus for its installation|
|US6102045 *||Dec 24, 1997||Aug 15, 2000||Premier Laser Systems, Inc.||Method and apparatus for lowering the intraocular pressure of an eye|
|US6143028 *||Apr 20, 1998||Nov 7, 2000||Galin; Miles A.||Medicament coated refractive anterior chamber ocular implant|
|US6203513||Nov 20, 1997||Mar 20, 2001||Optonol Ltd.||Flow regulating implant, method of manufacture, and delivery device|
|US6391052||Oct 29, 1997||May 21, 2002||Scimed Life Systems, Inc.||Stent with collagen|
|US6468283||Aug 26, 1999||Oct 22, 2002||Optonol, Ltd.||Method of regulating pressure with an intraocular implant|
|US6508779||Jan 24, 1997||Jan 21, 2003||John Suson||Adjustable flow rate glaucoma shunt and method of using same|
|US6510600||Dec 4, 2000||Jan 28, 2003||Optonol, Ltd.||Method for manufacturing a flow regulating implant|
|US6558342||Jun 2, 1999||May 6, 2003||Optonol Ltd.||Flow control device, introducer and method of implanting|
|US6595945||Jan 9, 2001||Jul 22, 2003||J. David Brown||Glaucoma treatment device and method|
|US6726664||Aug 6, 2001||Apr 27, 2004||Optonol Ltd.||Flow control device, introducer and method of implanting|
|US6881198||Jun 16, 2003||Apr 19, 2005||J. David Brown||Glaucoma treatment device and method|
|US7160264||Dec 16, 2003||Jan 9, 2007||Medtronic-Xomed, Inc.||Article and method for ocular aqueous drainage|
|US7291125||Nov 14, 2003||Nov 6, 2007||Transcend Medical, Inc.||Ocular pressure regulation|
|US7481816||Oct 27, 2003||Jan 27, 2009||Optonol Ltd.||Intraocular implant, delivery device, and method of implantation|
|US7670310||Dec 7, 2007||Mar 2, 2010||Optonol Ltd||Flow regulating implants|
|US7740604||Sep 24, 2007||Jun 22, 2010||Ivantis, Inc.||Ocular implants for placement in schlemm's canal|
|US7815592||Apr 22, 2008||Oct 19, 2010||Transcend Medical, Inc.||Ocular pressure regulation|
|US7837644 *||Nov 21, 2006||Nov 23, 2010||Innfocus, Llc||Glaucoma implant device|
|US7850638||Dec 14, 2010||Transcend Medical, Inc.||Ocular pressure regulation|
|US7862531||Jun 25, 2004||Jan 4, 2011||Optonol Ltd.||Flow regulating implants|
|US8034016||Dec 7, 2007||Oct 11, 2011||Optonol, Ltd.||Flow regulating implants and methods of implanting|
|US8079972 *||Dec 20, 2011||Schocket Stanley S||Implant for use in surgery for glaucoma and a method|
|US8109896||Feb 7, 2012||Optonol Ltd.||Devices and methods for opening fluid passageways|
|US8128588||Dec 22, 2006||Mar 6, 2012||Transcend Medical, Inc.||Ocular pressure regulation|
|US8167939||May 1, 2012||Transcend Medical, Inc.||Ocular implant with stiffness qualities, methods of implantation and system|
|US8172899||May 8, 2012||Transcend Medical, Inc.||Ocular implant with stiffness qualities, methods of implantation and system|
|US8262726||Oct 5, 2010||Sep 11, 2012||Transcend Medical, Inc.||Ocular implant with stiffness qualities, methods of implantation and system|
|US8267882||Sep 18, 2012||Ivantis, Inc.||Methods and apparatus for treating glaucoma|
|US8282592||May 6, 2010||Oct 9, 2012||Ivantis, Inc.||Glaucoma treatment method|
|US8308701||Nov 13, 2012||Aquesys, Inc.||Methods for deploying intraocular shunts|
|US8313454||Mar 26, 2010||Nov 20, 2012||Optonol Ltd.||Fluid drainage device, delivery device, and associated methods of use and manufacture|
|US8337509||Dec 25, 2012||Ivantis, Inc.||Methods and apparatus for delivering ocular implants into the eye|
|US8372026||Feb 3, 2012||Feb 12, 2013||Ivantis, Inc.||Ocular implant architectures|
|US8377122||Jan 27, 2010||Feb 19, 2013||Transcend Medical, Inc.||Ocular implant with stiffness qualities, methods of implantation and system|
|US8398672||Mar 19, 2013||Nitinol Devices And Components, Inc.||Method for anchoring a medical device|
|US8409239||Nov 25, 2009||Apr 2, 2013||Nitinol Devices And Components, Inc.||Medical device anchor and delivery system|
|US8414518||Mar 21, 2012||Apr 9, 2013||Ivantis, Inc.||Glaucoma treatment method|
|US8425449||Jul 9, 2010||Apr 23, 2013||Ivantis, Inc.||Ocular implants and methods for delivering ocular implants into the eye|
|US8444588||May 21, 2013||Transcend Medical, Inc.||Internal shunt and method for treating glaucoma|
|US8486000||Nov 12, 2004||Jul 16, 2013||Transcend Medical, Inc.||Ocular pressure regulation|
|US8486086||Nov 7, 2011||Jul 16, 2013||Optonol, Ltd||Flow regulating implant, method of manufacture, and delivery device|
|US8512404||Nov 20, 2007||Aug 20, 2013||Ivantis, Inc.||Ocular implant delivery system and method|
|US8529492||Dec 20, 2010||Sep 10, 2013||Trascend Medical, Inc.||Drug delivery devices and methods|
|US8529494||Sep 11, 2012||Sep 10, 2013||Ivantis, Inc.||Methods and apparatus for treating glaucoma|
|US8551166||Nov 19, 2012||Oct 8, 2013||Ivantis, Inc.||Methods and apparatus for delivering ocular implants into the eye|
|US8574294||Dec 16, 2010||Nov 5, 2013||Transcend Medical, Inc.||Ocular implant with stiffness qualities, methods of implantation and system|
|US8585629||Dec 8, 2011||Nov 19, 2013||Aquesys, Inc.||Systems for deploying intraocular shunts|
|US8617139||Jun 25, 2009||Dec 31, 2013||Transcend Medical, Inc.||Ocular implant with shape change capabilities|
|US8657776||Jun 14, 2011||Feb 25, 2014||Ivantis, Inc.||Ocular implants for delivery into the eye|
|US8663150||Dec 19, 2011||Mar 4, 2014||Ivantis, Inc.||Delivering ocular implants into the eye|
|US8663303||Nov 15, 2010||Mar 4, 2014||Aquesys, Inc.||Methods for deploying an intraocular shunt from a deployment device and into an eye|
|US8672870||Jul 17, 2008||Mar 18, 2014||Transcend Medical, Inc.||Ocular implant with hydrogel expansion capabilities|
|US8721656||Dec 22, 2006||May 13, 2014||Transcend Medical, Inc.||Glaucoma treatment device|
|US8721702||Nov 15, 2010||May 13, 2014||Aquesys, Inc.||Intraocular shunt deployment devices|
|US8728021||Dec 17, 2010||May 20, 2014||Transcend Medical, Inc.||Ocular pressure regulation|
|US8734377||Sep 23, 2008||May 27, 2014||Ivantis, Inc.||Ocular implants with asymmetric flexibility|
|US8734378||Sep 17, 2009||May 27, 2014||Transcend Medical, Inc.||Glaucoma treatment device|
|US8758289||Dec 17, 2010||Jun 24, 2014||Transcend Medical, Inc.||Ocular pressure regulation|
|US8758290||Dec 23, 2011||Jun 24, 2014||Aquesys, Inc.||Devices and methods for implanting a shunt in the suprachoroidal space|
|US8765210||Dec 8, 2011||Jul 1, 2014||Aquesys, Inc.||Systems and methods for making gelatin shunts|
|US8771218||Dec 17, 2010||Jul 8, 2014||Transcend Medical, Inc.||Ocular pressure regulation|
|US8801649||Oct 5, 2010||Aug 12, 2014||Transcend Medical, Inc.||Glaucoma treatment device|
|US8801766||Nov 15, 2010||Aug 12, 2014||Aquesys, Inc.||Devices for deploying intraocular shunts|
|US8808220||Oct 14, 2010||Aug 19, 2014||Transcend Medical, Inc.||Ocular pressure regulation|
|US8808222||Aug 22, 2013||Aug 19, 2014||Ivantis, Inc.||Methods and apparatus for delivering ocular implants into the eye|
|US8814819||Dec 16, 2010||Aug 26, 2014||Transcend Medical, Inc.||Glaucoma treatment device|
|US8828070||Nov 15, 2010||Sep 9, 2014||Aquesys, Inc.||Devices for deploying intraocular shunts|
|US8852136||Dec 8, 2011||Oct 7, 2014||Aquesys, Inc.||Methods for placing a shunt into the intra-scleral space|
|US8852137||Dec 23, 2011||Oct 7, 2014||Aquesys, Inc.||Methods for implanting a soft gel shunt in the suprachoroidal space|
|US8852256||Nov 15, 2010||Oct 7, 2014||Aquesys, Inc.||Methods for intraocular shunt placement|
|US8945038||May 17, 2013||Feb 3, 2015||Transcend Medical, Inc.||Internal shunt and method for treating glaucoma|
|US8961447||Feb 25, 2013||Feb 24, 2015||Ivantis, Inc.||Glaucoma treatment method|
|US8974511||Nov 15, 2010||Mar 10, 2015||Aquesys, Inc.||Methods for treating closed angle glaucoma|
|US9017276||Jul 26, 2013||Apr 28, 2015||Aquesys, Inc.||Shunt placement through the sclera|
|US9039650||Apr 7, 2014||May 26, 2015||Ivantis, Inc.||Ocular implants with asymmetric flexibility|
|US9050169||Jul 14, 2014||Jun 9, 2015||Ivantis, Inc.||Methods and apparatus for delivering ocular implants into the eye|
|US9066750||Jan 2, 2014||Jun 30, 2015||Ivantis, Inc.||Delivering ocular implants into the eye|
|US9066783||Aug 15, 2013||Jun 30, 2015||Ivantis, Inc.||Methods and apparatus for treating glaucoma|
|US9084662||Jan 17, 2007||Jul 21, 2015||Transcend Medical, Inc.||Drug delivery treatment device|
|US9089392||Aug 23, 2013||Jul 28, 2015||Transcend Medical, Inc.||Drug delivery devices and methods|
|US9095411||Nov 15, 2010||Aug 4, 2015||Aquesys, Inc.||Devices for deploying intraocular shunts|
|US9095413||Jun 3, 2014||Aug 4, 2015||Aquesys, Inc.||Intraocular shunt manufacture|
|US9113994||Jun 3, 2014||Aug 25, 2015||Aquesys, Inc.||Intraocular shunt manufacture|
|US9125723||Feb 19, 2013||Sep 8, 2015||Aquesys, Inc.||Adjustable glaucoma implant|
|US9155654||Feb 17, 2012||Oct 13, 2015||Glaukos Corporation||Ocular system with anchoring implant and therapeutic agent|
|US9155655||Dec 23, 2013||Oct 13, 2015||Ivantis, Inc.||Ocular implants for delivery into the eye|
|US9155656||Feb 10, 2014||Oct 13, 2015||Transcend Medical, Inc.||Delivery system for ocular implant|
|US9173774||Sep 11, 2012||Nov 3, 2015||Optonol Ltd.||Fluid drainage device, delivery device, and associated methods of use and manufacture|
|US9192516||Feb 26, 2014||Nov 24, 2015||Aquesys, Inc.||Intraocular shunt placement|
|US9211213||Apr 18, 2013||Dec 15, 2015||Ivantis, Inc.||Ocular implants and methods for delivering ocular implants into the eye|
|US9226852||Apr 21, 2015||Jan 5, 2016||Ivantis, Inc.||Methods and apparatus for delivering ocular implants into the eye|
|US9241832||Apr 18, 2013||Jan 26, 2016||Transcend Medical, Inc.||Delivery system for ocular implant|
|US9271869||Oct 7, 2014||Mar 1, 2016||Aquesys, Inc.||Intrascleral shunt placement|
|US9283065||Apr 1, 2013||Mar 15, 2016||Nitinol Devices And Components, Inc.||Medical device anchor and delivery system|
|US9283116||Apr 28, 2014||Mar 15, 2016||Aquesys, Inc.||Intraocular shunt deployment device|
|US9326891||May 15, 2013||May 3, 2016||Aquesys, Inc.||Methods for deploying intraocular shunts|
|US9351873||Mar 6, 2014||May 31, 2016||Transcend Medical, Inc.||Ocular pressure regulation|
|US9351874||Apr 22, 2015||May 31, 2016||Ivantis, Inc.||Methods and apparatus for delivering ocular implants into the eye|
|US9358156||Mar 11, 2013||Jun 7, 2016||Invantis, Inc.||Ocular implants for delivery into an anterior chamber of the eye|
|US20030079329 *||Dec 9, 2002||May 1, 2003||Ira Yaron||Flow regulating implant, method of manufacture, and delivery device|
|US20040073156 *||Jun 16, 2003||Apr 15, 2004||Brown J. David||Glaucoma treatment device and method|
|US20040088048 *||Oct 27, 2003||May 6, 2004||Jacob Richter||Intraocular implant, delivery device, and method of implantation|
|US20040193095 *||Jan 17, 2004||Sep 30, 2004||Shadduck John H.||Implants for treating ocular hypertension, methods of use and methods of fabrication|
|US20040260227 *||Dec 16, 2003||Dec 23, 2004||Lisk James R.||Article and method for ocular aqueous drainage|
|US20050107734 *||Nov 14, 2003||May 19, 2005||Coroneo Minas T.||Ocular pressure regulation|
|US20050267398 *||May 25, 2005||Dec 1, 2005||Dimitri Protopsaltis||Glaucoma shunt|
|US20050288617 *||Jun 25, 2004||Dec 29, 2005||Ira Yaron||Flow regulating implants|
|US20060079828 *||Apr 18, 2005||Apr 13, 2006||Brown J D||Glaucoma treatment device and method|
|US20060276739 *||Dec 19, 2005||Dec 7, 2006||Brown J D||Glaucoma treatment device and method|
|US20070118066 *||Nov 21, 2006||May 24, 2007||Leonard Pinchuk||Glaucoma Implant Device|
|US20070149915 *||Aug 23, 2006||Jun 28, 2007||Judith Yablonski||Internal shunt and method for treating glaucoma|
|US20070156079 *||Sep 14, 2006||Jul 5, 2007||Bg Implant, Inc.||Glaucoma Treatment Devices and Methods|
|US20070191863 *||Dec 22, 2006||Aug 16, 2007||De Juan Eugene Jr||Glaucoma Treatment Device|
|US20070233037 *||Jan 17, 2007||Oct 4, 2007||Gifford Hanson S Iii||Drug Delivery Treatment Device|
|US20080077071 *||Dec 7, 2007||Mar 27, 2008||Optonol Ltd.||Flow Regulating Implants|
|US20080125691 *||Dec 7, 2007||May 29, 2008||Optonol Ltd.||Flow regulating implants|
|US20080277332 *||May 11, 2007||Nov 13, 2008||Becton, Dickinson And Company||Micromachined membrane filter device for a glaucoma implant and method for making the same|
|US20090082860 *||Sep 23, 2008||Mar 26, 2009||Schieber Andrew T||Ocular Implants with Asymmetric Flexibility|
|US20090132040 *||Nov 20, 2007||May 21, 2009||Ivantis, Inc.||Ocular Implant Delivery System and Method|
|US20100100104 *||Nov 17, 2009||Apr 22, 2010||Aquesys, Inc.||Systems for reducing pressure in an organ|
|US20100119696 *||Nov 17, 2009||May 13, 2010||Aquesys, Inc.||Manufacture of an organ implant|
|US20100121248 *||Nov 17, 2009||May 13, 2010||Aquesys, Inc.||Apparatus for reducing pressure in an organ|
|US20100121249 *||Nov 17, 2009||May 13, 2010||Aquesys, Inc.||Methods for reducing pressure in an organ|
|US20100121342 *||Dec 7, 2009||May 13, 2010||Schieber Andrew T||Methods and Apparatus for Delivering Ocular Implants Into the Eye|
|US20100125237 *||Nov 20, 2008||May 20, 2010||Schocket Stanley S||Implant for use in surgery for glaucoma and a method|
|US20100137981 *||Jun 25, 2009||Jun 3, 2010||Silvestrini Thomas A||Ocular implant with shape change capabilities|
|US20100168644 *||Dec 23, 2009||Jul 1, 2010||Brown J David||Glaucoma Treatment Device and Method|
|US20100185138 *||Jan 21, 2010||Jul 22, 2010||Optonol Ltd.||Flow regulating implant, method of manufacture, and delivery device|
|US20100222733 *||Sep 2, 2010||Schieber Andrew T||Glaucoma Treatment Method|
|US20100274258 *||Jan 27, 2010||Oct 28, 2010||Silvestrini Thomas A||Ocular implant with stiffness qualities, methods of implantation and system|
|US20100274259 *||Mar 26, 2010||Oct 28, 2010||Optonol Ltd.||Fluid drainage device, delivery device, and associated methods of use and manufacture|
|US20110009874 *||Jan 13, 2011||John Wardle||Single Operator Device for Delivering an Ocular Implant|
|US20110009958 *||Jan 13, 2011||John Wardle||Ocular Implants and Methods for Delivering Ocular Implants Into the Eye|
|US20110028883 *||Oct 5, 2010||Feb 3, 2011||Juan Jr Eugene De||Glaucoma treatment device|
|US20110028884 *||Feb 3, 2011||Minas Theodore Coroneo||Ocular pressure regulation|
|US20110028983 *||Feb 3, 2011||Silvestrini Thomas A||Ocular implant with stiffness qualities, methods of implantation and system|
|US20110087148 *||Dec 16, 2010||Apr 14, 2011||Silvestrini Thomas A||Ocular implant with stiffness qualities, methods of implantation and system|
|US20110087149 *||Apr 14, 2011||Minas Theodore Coroneo||Ocular pressure regulation|
|US20110087151 *||Dec 17, 2010||Apr 14, 2011||Minas Theodore Coroneo||Ocular pressure regulation|
|US20110118745 *||Dec 9, 2010||May 19, 2011||Aquesys, Inc.||Methods, systems and apparatus for relieving pressure in an organ|
|US20110238075 *||Dec 20, 2010||Sep 29, 2011||Luke Clauson||Drug delivery devices and methods|
|WO1991012046A1 *||Feb 12, 1991||Aug 22, 1991||Atos Medical Ab||Glaucoma valve|
|WO1992019294A1 *||May 8, 1992||Nov 12, 1992||Prywes Arnold S||Shunt valve and therapeutic delivery systems|
|WO2002032343A2||Oct 18, 2001||Apr 25, 2002||Wilcox Michael J||C-shaped cross section tubular ophthalmic implant for reduction of intraocular pressure and method of use|
|U.S. Classification||604/8, 604/294|
|Cooperative Classification||A61F9/007, A61F9/00781|
|European Classification||A61F9/007, A61F9/007V|
|Dec 1, 1992||REMI||Maintenance fee reminder mailed|
|May 2, 1993||LAPS||Lapse for failure to pay maintenance fees|
|Jul 20, 1993||FP||Expired due to failure to pay maintenance fee|
Effective date: 19930502